Jiang Group - Selected Publications

  • Denker E, Sehring IM, Dong B, Audisso J, Mathiesen B, Jiang D. (2015). Regulation by a TGFβ-ROCK-actomyosin axis secures a non-linear lumen expansion that is essential for tubulogenesis. Development pii: dev.117150 - abstract

  • Sehring Y, Recho P, Denker E, Kourakis M, Mathiesen B, Hannezo E, Dong B, Jiang D (2015). Assembly and positioning of actomyosin rings by contractility and planar cell polarity.. eLife;10.7554/eLife.09206

  • Buisson N, Sirour C, Moreau N, Denker E, Le Bouffant R, Goullancourt A, Darribere T, Bello V (2014). An adhesome comprising laminin, dystroglycan and myosin IIA is required during notochord development in Xenopus laevis. Development 141 (23) 4569-79

  • Sehring IM, Dong B, Denker E, Bhattachan P, Deng W, Mathiesen BT, Jiang D (2014). An Equatorial Contractile Mechanism Drives Cell Elongation but not Cell Division PLoS Biol. 12(2):e1001781. doi: 10.1371/journal.pbio.1001781.

  • Deng W, Niesb F, Feuerb A, Bocinac I, Oliverb D, and Di Jiang (2013) Anion translocation through an Slc26 transporter mediates lumen expansion during tubulogenesis. Proc. Natl. Acad. Sci. U. S. A. doi: 10.1073/pnas.1220884110.

  • Denker E, Boina A, Jiang D (2013). Tubulogenesis in a simple cell cord requires the formation of bi-apical cells through two discrete Par domains. Development 140(14):2985-96. doi: 10.1242/dev.092387. Epub 2013 Jun 12.

  • Denker E, Jiang D (2012). Ciona intestinalis notochord as a new model to investigate the cellular and molecular mechanisms of tubulogenesis. Semin. Cell Dev. Biol. May;23(3):308-19. Epub 2012 Mar 23. Review

  • Sommer F, Awazu S, Anton-Erxleben F, Jiang D, Klimovich AV, Klimovich BV, Samoilovich MP, Satou Y, Krüss M, Gelhaus C, Kürn U, Bosch TC and Khalturin K (2012). Blood System Formation in the Urochordate Ciona intestinalis Requires the Variable Receptor vCRL1. Mol. Biol. Evol. Oct;29(10):3081-93. Epub 2012 Apr 18.

  • José-Edwards DS, Kerner P, Kugler JE, Deng W, Jiang D, Di Gregorio A (2011). The identification of transcription factors expressed in the notochord of Ciona intestinalis adds new potential players to the brachyury gene regulatory network. Dev Dyn., 240(7):1793-1805. doi: 10.1002/dvdy.22656. Epub 2011 May 18.

  • Dong B, Deng W, Jiang D (2011). Distinct cytoskeleton population and extensive crosstalks control the Ciona notochord tubulogenesis. Development 138 (8):1631-1641.

  • Kugler JE, Kerner P, Bouquet JM, Jiang D, Di Gregorio A (2011). Evolutionary changes in the notochord genetic toolkit: a comparative analysis of notochord genes in the ascidian Ciona intestinalis ant the larvacean Oikopleura dioiac. BMC Evol. Biol. 11:21-36.

  • Dong B, Horie T, Denker E, Kusakabe T, Tsuda M, Smith WC, Jiang D (2009). Tube formation by complex cellular processes in Ciona intestinalis notochord. Dev Biol. 330(2):237-49.

  • Chiba S, Jiang D, Satoh N, Smith WC (2009). Brachyury null mutant-induced defects in juvenile ascidian endodermal organs. Development 136(1):35-9.

  • Hill MM, Broman KW, Stupka E, Smith WC, Jiang D, Sidow A (2008). The C. savignyi genetic map and its integration with the reference sequence facilitates insights into chordate genome evolution. Genome Res. 18(8):1369-79.

  • Jiang D, Smith WC. (2007) Ascidian notochord morphogenesis. Dev Dyn. 236(7):1748-57. Review.

  • Jiang D, Smith WC. (2005) Self and cross-fertilization in the solitary ascidian Ciona savignyi. Biol Bull, 209(2):107-12.

  • Jiang D, Munro EM, Smith WC. (2005) Ascidian prickle regulates both mediolateral and anterior-posterior cell polarity of notochord cells. Current Biology, 11;15(1):79-85.

  • Jiang D, Tresser JW, Horie T, Tsuda M, Smith WC. (2005) Pigmentation in the sensory organs of the ascidian larva is essential for normal behavior. J Exp Biol 1;208(3):433-8.

  • Hendrickson C, Christiaen L, Deschet K, Jiang D, Joly JS, Legendre L, Nakatani Y, Tresser J, Smith WC. (2004) Culture of adult ascidians and ascidian genetics. Methods Cell Biol, 74:143-70. Review.

  • Jiang D, Smith WC. (2002) An ascidian engrailed gene. Dev Genes Evol, 212(8):399-402.

  • Kim CH, Oda T, Itoh M, Jiang D, Artinger KB, Chandrasekharappa SC, Driever W, Chitnis AB. (2000) Repressor activity of Headless/Tcf3 is essential for vertebrate head formation. Nature 19;407(6806):913-6.

  • Jiang D, Zheng L, Lenardo MJ. (1999) Caspases in T-cell receptor-induced thymocyte apoptosis. Cell Death Differ 6(5):402-11.

  • Martin DA, Combadiere B, Hornung F, Jiang D, McFarland H, Siegel R, Trageser C, Wang J, Zheng L, Lenardo MJ. (1998) Molecular genetic studies in lymphocyte apoptosis and human autoimmunity. Novartis Found Symp, 215:73-82; discussion 82-91. Review.

  • Albright JW, Jiang D, Albright JF. (1997) Innate control of the early course of infection in mice inoculated with Trypanosoma musculi. Cell Immunol 15;176(2):146-52.

  • Jiang D, Lenardo MJ, Zuniga-Pflucker JC. (1996) p53 prevents maturation to the CD4+CD8+ stage of thymocyte differentiation in the absence of T cell receptor rearrangement. J Exp Med 1;183(4):1923-8.

  • Zuniga-Pflucker JC, Jiang D, Lenardo MJ. (1995) Requirement for TNF-alpha and IL-1 alpha in fetal thymocyte commitment and differentiation. Science 30;268(5219):1906-9.

  • Zuniga-Pflucker JC, Jiang D, Schwartzberg PL, Lenardo MJ. (1994) Sublethal gamma-radiation induces differentiation of CD4-/CD8- into CD4+/CD8+ thymocytes without T cell receptor beta rearrangement in recombinase activation gene 2-/- mice. J Exp Med 1;180(4):1517-21.

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